Evidence map›Paper›PMID 11526491›Full record

ArticleOncogene2001

No evidence of somatic FGFR3 mutation in various types of carcinoma.

M Karoui, H Hofmann-Radvanyi, U Zimmermann, A Couvelard, C Degott, L Faridoni-Laurens, J C Ahomadegbe, S Gazzeri, E Brambilla, T Clerici and 10 more

Abstract read
PubMed Publisher
In one paragraph

Article in Oncogene, 2001. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
0.9field-weighted citation impact, top 27% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

14 citing papers in PubMed, 45 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. A genomics-based classification of human lung tumors.Science translational medicine · 2013
    Article
  5. Article
  6. Article
  7. Overexpression of KLF13 and FGFR3 in oral cancer cells.Cytogenetic and genome research · 2010
    Article
  8. Review
  9. Article
  10. Article
  11. Article
  12. Review
  13. Article
  14. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

20 authors at 5 institutions in 1 country.

M KarouiFédération des Spécialités Digestives, Hôpital Ambroise Paré, Université Paris V, 92104 Boulogne Cedex, France.
H Hofmann-Radvanyi
U Zimmermann
A Couvelard
C Degott
L Faridoni-Laurens
J C Ahomadegbe
S Gazzeri
E Brambilla
T Clerici
P Charbonnier
C Tresallet
E Mitry
C Penna
P Rougier
C Boileau
J P Thiery
B Nordlinger
B Franc
F Radvanyi
Université Paris Cité · FRCentre National de la Recherche Scientifique · FRCentre Hospitalier Universitaire de Grenoble · FRHôpital Beaujon · FRInstitut Gustave Roussy · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Germline specific point mutations in the gene encoding fibroblast growth factor receptor 3 (FGFR3) are associated with autosomal dominant human skeletal dysplasia and craniosynostosis syndromes. Mutations identical to the germinal activating mutations found in severe skeletal dysplasias have been identified in certain types of cancer: at low frequency in multiple myeloma and cervix carcinoma and at high frequency in bladder carcinoma. We analysed, by SSCP and sequencing, the prevalence of FGFR3 mutations in 116 primary tumours of various types (upper aerodigestive tract, oesophagus, stomach, lung and skin). The regions analysed encompassed all FGFR3 point mutations previously described in severe skeletal dysplasia and cancers. No mutations were detected in the tumour types examined, suggesting that FGFR3 mutations are restricted to a few tumour types, the evidence to date suggesting that they are very specific to bladder carcinomas.

Indexed as

Bone Diseases, DevelopmentalCarcinomaHumansOncogenesPoint MutationPolymorphism, Single-Stranded ConformationalReceptors, Fibroblast Growth FactorUrinary Bladder NeoplasmsReceptors, Fibroblast Growth Factor

Identifiers

PMID11526491
OpenAlexW2080988586

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.